Taiwan FDA registration 34721241f42b1618dc687a096f55eb75
“GENEMAX” Mechanical walker(Non-Sterile)
TW: “吉律”機械式助行器(未滅菌)
Taiwan·Risk Class 1·MD·GENEMAX MEDICAL PRODUCTS INDUSTRY CORP.·Registered Apr 08, 2021 – Apr 08, 2026ExpiredRegistration details
- Analysis ID
- 34721241f42b1618dc687a096f55eb75
- License Form
- Ministry of Health Medical Device Manufacturing No. 008997
Company information
- Manufacturer
- GENEMAX MEDICAL PRODUCTS INDUSTRY CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENEMAX MEDICAL PRODUCTS INDUSTRY CORP.
Product details
- Intended Use
- Limited to the scope of Grade 1 identification of "Mechanical Mobility Aids (O.3825)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3825 Mechanical Mobility Aid
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 08, 2021
- Expiry Date
- Apr 08, 2026
About this record
Access comprehensive regulatory information for “GENEMAX” Mechanical walker(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 34721241f42b1618dc687a096f55eb75 and manufactured by GENEMAX MEDICAL PRODUCTS INDUSTRY CORP.. The authorized representative in Taiwan is GENEMAX MEDICAL PRODUCTS INDUSTRY CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices